MEDLIB
Orphanet Datenbank

Seltene Erkrankungen

7,547 Erkrankungen mit Genetik, Phänotypen und Epidemiologie

7,547Erkrankungen
4 552Gene
8 700Phänotypen
3,968 Erkrankungen gefunden (Kr.) Zurücksetzen

Paratyphoid fever

ORPHA:443227Kr.
Not applicable

Paris-Trousseau thrombocytopenia

ORPHA:851Kr.

Parkes Weber syndrome

ORPHA:90307Kr.
Autosomal dominant, Not applicable

Parkinson-dementia complex of Guam

ORPHA:90020Kr.

Parkinsonian-pyramidal syndrome

ORPHA:171695Kr.
Autosomal recessive

Parkinsonism with polyneuropathy

ORPHA:611237Kr.

Paroxysmal cold hemoglobinuria

ORPHA:90035Kr.
Multigenic/multifactorial

Paroxysmal dystonic choreathetosis with episodic ataxia and spasticity

ORPHA:53583Kr.
Autosomal dominant

Paroxysmal exertion-induced dyskinesia

ORPHA:98811Kr.
Autosomal dominant, Not applicable

Paroxysmal extreme pain disorder

ORPHA:46348Kr.
Autosomal dominant

Paroxysmal hemicrania

ORPHA:157835Kr.
Not applicable

Paroxysmal kinesigenic dyskinesia

ORPHA:98809Kr.
Autosomal dominant, Not applicable

Paroxysmal nocturnal hemoglobinuria

ORPHA:447Kr.
Not applicable

Paroxysmal non-kinesigenic dyskinesia

ORPHA:98810Kr.
Autosomal dominant, Not applicable

Partial androgen insensitivity syndrome

ORPHA:90797Kr.
X-linked recessive

Partially involuting congenital hemangioma

ORPHA:458785Kr.
Not applicable

Pauci-immune glomerulonephritis

ORPHA:93126Kr.
Not applicable

Pearson syndrome

ORPHA:699Kr.
Mitochondrial inheritance, Not applicable

Pediatric acute respiratory distress syndrome

ORPHA:685082Kr.

Pediatric collagenous gastritis

ORPHA:487809Kr.

Pediatric hepatocellular carcinoma

ORPHA:33402Kr.
Not applicable

Pediatric multiple sclerosis

ORPHA:477738Kr.

Pediatric systemic lupus erythematosus

ORPHA:93552Kr.
Not applicable

Pediatric-onset Graves disease

ORPHA:525731Kr.